Alkaline degradation of lyophilized DMSA prior to labeling with 99mTc

dc.contributor.authorALMEIDA, ERIKA V.
dc.contributor.authorBRITO, SAMUEL L. de
dc.coverageInternacionalpt_BR
dc.date.accessioned2018-07-11T12:55:41Z
dc.date.available2018-07-11T12:55:41Z
dc.date.issued2018pt_BR
dc.description.abstractIntroduction: Complexes of technetium-99m (Tc-99m) with meso-dimercaptosuccinic acid (DMSA) have been widely used as diagnostic agents in nuclear medicine. The degradation products (DP) of DMSA formed under different forced conditions have been identified through HPLC-DAD and LC-MSn studies. In this study, the DMSA kit was subjected to forced degradation under hydrolysis conditions as prescribed by the International Conference on Harmonization (ICH) guideline Q1A. Methods: Chromatographic separation was accomplished on a reverse phase Shim-Pack VP-ODS (150 mm x 4.6 mm; 5 pm) analytical column using the gradient elution method. LC-MSn analysis was performed using an Esquire 3000 Plus ion trap mass spectrometer, operating under electrospray ionization (ESI). Results: No products were found under acidic or neutral stress conditions. All the products found were identified through LC-MSn analyses and their fragmentation pathways were proposed. The DMSA standard degraded into an adduct DMSA dimer (2DMSA[-2H + Na](+)) and adduct DMSA bound to fumaric acid and dithioglucolic acid (DTGA). In the DMSA kit, the degradation products were dimers and trimers of DMSA with tin. A possible degradation pathway is presented. Conclusions: This method proved to be convenient and effective since it provided fast and efficient separation of DMSA from its degradation products. The degradation studies carried out were able to delineate the stability of the DMSA standard and the DMSA kit.pt_BR
dc.format.extent20-27pt_BR
dc.identifier.citationALMEIDA, ERIKA V.; BRITO, SAMUEL L. de. Alkaline degradation of lyophilized DMSA prior to labeling with 99mTc: identification and development of the degradation pathway by HPLC and MS. <b>Nuclear Medicine and Biology</b>, v. 57, p. 20-27, 2018. DOI: <a href="https://dx.doi.org/10.1016/j.nucmedbio.2017.11.002">10.1016/j.nucmedbio.2017.11.002</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/28917.
dc.identifier.doi10.1016/j.nucmedbio.2017.11.002pt_BR
dc.identifier.issn0969-8051pt_BR
dc.identifier.percentilfi57.75en
dc.identifier.percentilfiCiteScore60.00
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/28917
dc.identifier.vol57pt_BR
dc.relation.ispartofNuclear Medicine and Biologypt_BR
dc.rightsopenAccesspt_BR
dc.subjecttechnetium 99
dc.subjectradiopharmaceuticals
dc.subjectsuccinic acid
dc.subjecthigh-performance liquid chromatography
dc.subjectmass spectroscopy
dc.subjectnuclear medicine
dc.subjectalkaline hydrolysis
dc.subjectlyophilization
dc.titleAlkaline degradation of lyophilized DMSA prior to labeling with 99mTcpt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorSAMUEL DE BRITO LEVINDO
ipen.autorERIKA VIEIRA DE ALMEIDA
ipen.codigoautor10917
ipen.codigoautor6578
ipen.contributor.ipenauthorSAMUEL DE BRITO LEVINDO
ipen.contributor.ipenauthorERIKA VIEIRA DE ALMEIDA
ipen.date.recebimento18-07pt_BR
ipen.identifier.fi2.492pt_BR
ipen.identifier.fiCiteScore4.6
ipen.identifier.ipendoc24700pt_BR
ipen.identifier.iwosWoSpt_BR
ipen.range.fi1.500 - 2.999
ipen.range.percentilfi50.00 - 74.99
ipen.subtituloidentification and development of the degradation pathway by HPLC and MSpt_BR
ipen.type.genreArtigo
relation.isAuthorOfPublication2c4cd9e9-3fd4-44ad-88f9-9b344f843079
relation.isAuthorOfPublicationed499d5b-4517-46f9-ab0e-aba66afdbf80
relation.isAuthorOfPublication.latestForDiscoveryed499d5b-4517-46f9-ab0e-aba66afdbf80
sigepi.autor.atividadeALMEIDA, ERIKA V.:6578:-1:Spt_BR
sigepi.autor.atividadeBRITO, SAMUEL L. DE:10917:-1:N

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